4.2 Article

Potential Ameliorative Effects of Qing Ye Dan Against Cadmium Induced Prostatic Deficits via Regulating Nrf-2/HO-1 and TGF-β1/Smad Pathways

期刊

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
卷 43, 期 4, 页码 1359-1368

出版社

KARGER
DOI: 10.1159/000481847

关键词

Cadmium; Prostate; Qing Ye Dan; Transforming growth factor-beta 1; Nuclear related factor-2

资金

  1. Natural Science Fund of Health and Family Planning Commission of Wuhan Municipality, China [WZ17Q05]
  2. State Natural Sciences Fund of China [81603177]
  3. Hubei Province health and family planning scientific research project [WJ2017M189]
  4. Youth Science and Technology Plan of Wuhan, China [2015071704011629]

向作者/读者索取更多资源

Background/Aims: Cadmium (Cd) is an environmental pollutant with reproductive toxicity. Swertia mileensis is used in Chinese medicine for the treatment of prostatic deficits and named as Qing Ye Dan (QYD). This study was undertaken to investigate the potential protective effects of QYD against Cd-induced prostatic deficits. Method: Rat model of prostatic deficits was induced by 0.2 mg/kg/d CdCl2 subcutaneous injection for 15 days. The prostatic oxidative stress was evaluated by detecting the levels of malondialdehyde, nitric oxide, reduced/oxidized glutathione, total sulfhydryl groups and enzymatic antioxidant status. The prostatic inflammation was estimated by testing the levels of pro-inflammatory cytokines. The levels of epithelial-mesenchymal transition (EMT) markers E-cadherin, fibronectin, vimentin and alpha-smooth muscle actin were measured by qPCR analysis. Additionally, the prostatic expressions of transforming growth factor-beta 1 (TGF-beta 1), type I TGF-beta receptor (TGF-beta RI), Smad2, phosphorylation-Smad2 (p-Smad2), Smad3, p-Smad3, Smad7, nuclear related factor-2 (Nrf2), heme oxygenase-1 (HO-1), B-cell CLL/lymphoma (Bcl)-2 and Bcl-2-associated X protein (Bax) were measured by western blot assay. Results: It was found that QYD ameliorated the Cd-induced prostatic oxidative stress and inflammation, attenuated prostatic EMT, inhibited the TGF-beta 1/Smad pathway, increased Bcl-2/Bax ratio and enhanced the activity of Nrf-2/HO-1 pathway. Conclusion: These results showed that QYD could ameliorate Cd-induced prostatic deficits via modulating Nrf-2/HO-1 and TGF-beta 1/Smad pathways.

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